Power to detect risk alleles using genome-wide tag SNP panels.

doi:10.1371/journal.pgen.0030170

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Back to search

Article

Power to detect risk alleles using genome-wide tag SNP panels.

PLoS genetics - 1 Oct 2007

Eberle Michael A, Ng Pauline C, Kuhn Kenneth, Zhou Lixin, Peiffer Daniel A, Galver Luana, Viaud-Martinez Karine A, Lawley Cynthia Taylor, Gunderson Kevin L, Shen Richard, Murray Sarah S

Abstract excerpt

Advances in high-throughput genotyping and the International HapMap Project have enabled association studies at the whole-genome level. We have constructed whole-genome genotyping panels of over 550,000 (HumanHap550) and 650,000 (HumanHap650Y) SNP loci by choosing tag SNPs from all populations genotyped by the International HapMap Project. These panels also contain additional SNP content in regions that have...

Topics

Alleles
Genome, Human
Haploidy
Humans
Polymorphism, Single Nucleotide
Risk Factors

Source

Open in PubMed Open full text

Identifiers

PMID: 17922574
DOI: 10.1371/journal.pgen.0030170
PMCID: PMC2000969

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

discussions

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics